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Induction of Pluripotency in Adult Equine Fibroblasts without c-MYC

机译:没有c-MYC的成年马成纤维细胞多能性的诱导

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Despite tremendous efforts on isolation of pluripotent equine embryonic stem (ES) cells, to date there are few reports about successful isolation of ESCs and no report ofin vivodifferentiation of this important companion species. We report the induction of pluripotency in adult equine fibroblasts via retroviral transduction with three transcription factors usingOCT4, SOX2, andKLF4in the absence of c-MYC. The cell lines were maintained beyond 27 passages (more than 11 months) and characterized. The equine iPS (EiPS) cells stained positive for alkaline phosphatase by histochemical staining and expressed OCT4, NANOG, SSEA1, and SSEA4. Gene expression analysis of the cells showed the expression ofOCT4, SOX2 NANOG, andSTAT3. The cell lines retained a euploid chromosome count of 64 after long-term culture cryopreservation. The EiPS demonstrated differentiation capacity for the three embryonic germ layers bothin vitroby embryoid bodies (EBs) formation andin vivoby teratoma formation. In conclusion, we report the derivation of iPS cells from equine adult fibroblasts and long-term maintenance using either of the three reprogramming factors.
机译:尽管在分离多能马胚胎干(ES)细胞方面做出了巨大努力,但迄今为止,很少有关于成功分离ESC的报道,也没有关于该重要伴侣物种的体内分化的报道。我们报道了在不存在c-MYC的情况下,通过使用OCT4,SOX2和KLF4的三个转录因子的逆转录病毒转导,在成年马成纤维细胞中诱导多能性。维持细胞系超过27代(超过11个月)并进行表征。马iPS(EiPS)细胞通过组织化学染色染色为碱性磷酸酶阳性,并表达OCT4,NANOG,SSEA1和SSEA4。细胞的基因表达分析显示了OCT4,SOX2 NANOG和STAT3的表达。长期培养冷冻保存后,细胞系保留了整倍体染色体数64。 EiPS证明了体外通过胚状体(EBs)形成和体内通过畸胎瘤形成对三个胚芽层的分化能力。总之,我们报告了使用三种重编程因子之一从马成人成纤维细胞衍生iPS细胞并进行长期维护。

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